Sterically oriented synthesis and structure of new perphosphorylated resorcinarenes View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2008-03

AUTHORS

V. I. Maslennikova, O. S. Serkova, T. V. Guzeeva, L. K. Vasyanina, K. A. Lysenko, V. V. Kopteva, E. E. Nifant’ev

ABSTRACT

Tetraarylresorcinarenes in a chair conformation of C2h symmetry were synthesized by sterically oriented condensation of aromatic aldehydes with resorcinol and 2-methylresorcinol. By further phosphorylation of resorcinarenes with phosphorous amides perphosphorylated derivatives were obtained with rctt configuration of substituents at internuclear methylidene bridges. Structure of these compounds was proved using NMR spectroscopy and X-ray diffraction analysis. More... »

PAGES

392-401

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363208030092

DOI

http://dx.doi.org/10.1134/s1070363208030092

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1035557446


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